Canonical Allele Identifier: CA916107879
Gene: C1orf127 HGNC NCBI

Linked Data

dbSNP Id: rs111510981

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10972920_10972921del , CM000663.2:g.10972920_10972921del GRCh38
NC_000001.10:g.11032977_11032978del , CM000663.1:g.11032977_11032978del GRCh37
NC_000001.9:g.10955564_10955565del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377004.9:c.128-2826_128-2825del MANE Select ENSP00000366203.4:n.128-2826_128-2825del
ENST00000377004.8:c.128-2826_128-2825del ENSP00000366203.4:n.128-2826_128-2825del
ENST00000520253.1:c.61-2826_61-2825del
NM_001170754.1:c.128-2826_128-2825del NP_001164225.1:n.128-2826_128-2825del
NM_001170754.2:c.128-2826_128-2825del MANE Select NP_001164225.1:n.128-2826_128-2825del